ENST00000205402.10:c.1429T>A
MANE Select
|
ENSP00000205402.3:p.Cys477Ser
|
|
ENST00000205402.9:c.1429T>A
|
ENSP00000205402.3:p.Cys477Ser
|
|
ENST00000415325.5:c.*1103T>A
|
ENSP00000402593.1:n.*1103T>A
|
|
ENST00000417551.5:c.1429T>A
|
ENSP00000390667.1:p.Cys477Ser
|
|
ENST00000437604.6:c.1285T>A
|
ENSP00000387542.2:p.Cys429Ser
|
|
ENST00000440410.5:c.1360T>A
|
ENSP00000417016.1:p.Cys454Ser
|
|
NM_000108.4:c.1429T>A
|
NP_000099.2:p.Cys477Ser
|
|
NM_001289750.1:c.1132T>A
|
NP_001276679.1:p.Cys378Ser
|
|
NM_001289751.1:c.1360T>A
|
NP_001276680.1:p.Cys454Ser
|
|
NM_001289752.1:c.1285T>A
|
NP_001276681.1:p.Cys429Ser
|
|
NM_000108.5:c.1429T>A
MANE Select
|
NP_000099.2:p.Cys477Ser
|
|